Home NDC 68001-440-00 Fexofenadine hydrochloride
Product NDC 68001-440
Requested package NDC 68001-440-00
11-digit product format 680010440
Labeler code 68001
Product ID 68001-440_bd31cd71-9281-7667-e053-2995a90a4ac0
Type HUMAN OTC DRUG
Nonproprietary name Fexofenadine hydrochloride
Dosage form TABLET
Route ORAL
Labeler BluePoint Laboratories
Application ANDA076502
Marketing category ANDA
Marketing start 2020-06-19
Substance FEXOFENADINE HYDROCHLORIDE
Active strength 180 mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Source provenance: Browse the complete Orange Book source catalog · source snapshot 42 .
Orange Book products# Current product rows page 1 of 1 · 9 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A076502-001 FEXOFENADINE HYDROCHLORIDE FEXOFENADINE HYDROCHLORIDE 30MG TABLET / ORAL 2006-04-11 A076502-002 FEXOFENADINE HYDROCHLORIDE FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL 2006-04-11 A076502-003 FEXOFENADINE HYDROCHLORIDE FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL 2006-04-11 A076502-004 CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY FEXOFENADINE HYDROCHLORIDE 30MG TABLET / ORAL 2011-04-12 A076502-005 CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES FEXOFENADINE HYDROCHLORIDE 30MG TABLET / ORAL 2011-04-12 A076502-006 FEXOFENADINE HYDROCHLORIDE ALLERGY FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL 2011-04-12 A076502-007 FEXOFENADINE HYDROCHLORIDE HIVES FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL 2011-04-12 A076502-008 FEXOFENADINE HYDROCHLORIDE ALLERGY FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL 2011-04-12 A076502-009 FEXOFENADINE HYDROCHLORIDE HIVES FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL 2011-04-12
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 1 of 10 · 378 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-08-18 06:07:40 2026-07 A076502-001 FEXOFENADINE HYDROCHLORIDE 30MG TABLET / ORAL 2006-04-11 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A076502-002 FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL 2006-04-11 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A076502-003 FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL 2006-04-11 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A076502-004 CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY 30MG TABLET / ORAL 2011-04-12 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A076502-005 CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES 30MG TABLET / ORAL 2011-04-12 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A076502-006 FEXOFENADINE HYDROCHLORIDE ALLERGY 60MG TABLET / ORAL 2011-04-12 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A076502-007 FEXOFENADINE HYDROCHLORIDE HIVES 60MG TABLET / ORAL 2011-04-12 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A076502-008 FEXOFENADINE HYDROCHLORIDE ALLERGY 180MG TABLET / ORAL 2011-04-12 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A076502-009 FEXOFENADINE HYDROCHLORIDE HIVES 180MG TABLET / ORAL 2011-04-12 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A076502-001 FEXOFENADINE HYDROCHLORIDE 30MG TABLET / ORAL AB 2006-04-11 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A076502-002 FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL AB 2006-04-11 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A076502-003 FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL AB 2006-04-11 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A076502-004 CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY 30MG TABLET / ORAL 2011-04-12 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A076502-005 CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES 30MG TABLET / ORAL 2011-04-12 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A076502-006 FEXOFENADINE HYDROCHLORIDE ALLERGY 60MG TABLET / ORAL 2011-04-12 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A076502-007 FEXOFENADINE HYDROCHLORIDE HIVES 60MG TABLET / ORAL 2011-04-12 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A076502-008 FEXOFENADINE HYDROCHLORIDE ALLERGY 180MG TABLET / ORAL 2011-04-12 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A076502-009 FEXOFENADINE HYDROCHLORIDE HIVES 180MG TABLET / ORAL 2011-04-12 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076502-001 FEXOFENADINE HYDROCHLORIDE 30MG TABLET / ORAL AB 2006-04-11 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076502-002 FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL AB 2006-04-11 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076502-003 FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL AB 2006-04-11 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076502-004 CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY 30MG TABLET / ORAL 2011-04-12 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076502-005 CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES 30MG TABLET / ORAL 2011-04-12 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076502-006 FEXOFENADINE HYDROCHLORIDE ALLERGY 60MG TABLET / ORAL 2011-04-12 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076502-007 FEXOFENADINE HYDROCHLORIDE HIVES 60MG TABLET / ORAL 2011-04-12 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076502-008 FEXOFENADINE HYDROCHLORIDE ALLERGY 180MG TABLET / ORAL 2011-04-12 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A076502-009 FEXOFENADINE HYDROCHLORIDE HIVES 180MG TABLET / ORAL 2011-04-12 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A076502-001 FEXOFENADINE HYDROCHLORIDE 30MG TABLET / ORAL AB 2006-04-11 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A076502-002 FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL AB 2006-04-11 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A076502-003 FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL AB 2006-04-11 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A076502-004 CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY 30MG TABLET / ORAL 2011-04-12 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A076502-005 CHILDREN'S FEXOFENADINE HYDROCHLORIDE HIVES 30MG TABLET / ORAL 2011-04-12 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A076502-006 FEXOFENADINE HYDROCHLORIDE ALLERGY 60MG TABLET / ORAL 2011-04-12 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A076502-007 FEXOFENADINE HYDROCHLORIDE HIVES 60MG TABLET / ORAL 2011-04-12 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A076502-008 FEXOFENADINE HYDROCHLORIDE ALLERGY 180MG TABLET / ORAL 2011-04-12 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A076502-009 FEXOFENADINE HYDROCHLORIDE HIVES 180MG TABLET / ORAL 2011-04-12 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A076502-001 FEXOFENADINE HYDROCHLORIDE 30MG TABLET / ORAL AB 2006-04-11 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A076502-002 FEXOFENADINE HYDROCHLORIDE 60MG TABLET / ORAL AB 2006-04-11 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A076502-003 FEXOFENADINE HYDROCHLORIDE 180MG TABLET / ORAL AB 2006-04-11 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A076502-004 CHILDREN'S FEXOFENADINE HYDROCHLORIDE ALLERGY 30MG TABLET / ORAL 2011-04-12 fd3edfee7708…
Observed Orange Book normalized TE history# Normalized TE history page 1 of 3 · 120 observed states.
Additional Listing Data#
Finished product Yes
Brand name base Fexofenadine hydrochloride
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FEXOFENADINE HYDROCHLORIDE 180 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2S068B75ZU Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 997420 Internal RxNorm lookup 997501 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 68001-440-00 Fexofenadine hydrochloride 1 in 1 CARTON TABLET 1 2 68001-440-00 Fexofenadine hydrochloride 100 in 1 BOTTLE TABLET 100 2 68001-440-04 Fexofenadine hydrochloride 1 in 1 CARTON TABLET 1 2 68001-440-04 Fexofenadine hydrochloride 30 in 1 BOTTLE TABLET 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68001-440 FEXOFENADINE HYDROCHLORIDE TABLET [BLUEPOINT LABORATORIES] 2 Current NDC, Legacy NDC, 4 package rows 20210317_a86aebd0-937e-5d73-e053-2995a90a656a.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 18 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68001-440-00 68001044000 1 BOTTLE in 1 CARTON (68001-440-00) / 100 TABLET in 1 BOTTLE 1 bottle 2020-06-19 0000-00-00 No No Current